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1 l as surfaced other kinases that it potently inhibits.
2 oised to apoptose when survival pathways are inhibited.
3 e and consider how they might be modified or inhibited.
4 ed most frequently where acidic groundwaters inhibited (210)Pb readsorption (felsic-crystalline rocks
5 n, sodium aurothiomalate and aurothioglucose inhibited 48 clinical isolates of N. gonorrhoeae includi
8 llowing challenge and elicit antibodies that inhibit A. phagocytophilum cellular infection in vitro T
9 allenge groups, but not from control groups, inhibited A. phagocytophilum infection of HL-60 cells.
17 ased protective proinflammatory response and inhibited amastigote multiplication in infected J774 mac
18 , and activation levels and show that Zn(2+) inhibits AMPARs in an activity-dependent manner, opening
19 uction of the peripheral avascular retina to inhibit angiogenic stimuli to anti-VEGF agents, which in
21 an anti-AQP3 monoclonal antibody (mAb) that inhibited AQP3-facilitated H(2)O(2) and glycerol transpo
22 s bind in the active site and how ethambutol inhibits arabinosyltransferases by binding to the same s
25 ctions along the genome, translation must be inhibited at a defined point following infection to clea
26 ubset of the antibodies was able to potently inhibit authentic SARS-CoV-2 infection at a concentratio
27 I (CFA/I) fimbriae from Escherichia coli can inhibit autoimmune diseases in murine models by inducing
28 that BBR antagonizes beta-catenin pathway by inhibiting beta-catenin translation and mTOR activity an
29 o inhibition, whereas the bivalent IgG fully inhibits beta-tryptase activity in a hinge-dependent man
31 omain protein 1 (EPAS1 encoding HIF-2alpha), inhibited both distinct and overlapping transcriptional
38 variants display much lower activity and are inhibited by high concentrations of H(2)O(2) upon adsorp
39 %), and increased precipitation (+73.1%) but inhibited by increased drought (-30.4%), N deposition (-
41 recombinant DSG1; these IgG1 antibodies were inhibited by LJM17, LJM11, and DSG1 in a dose-dependent
42 ndent and saturable and can be competitively inhibited by mannose 6-phosphate, suggesting cation-inde
43 ity is increased by nutrient deprivation and inhibited by overnutrition, inflammation, and hypersecre
46 lutarate) as an obligate cosubstrate and are inhibited by succinate, fumarate, and 2-hydroxyglutarate
47 lectron pair donors: KPC-2 is preferentially inhibited by sulfonamide and tetrazole-based derivatives
49 hat the Drosophila PLK Polo kinase (Polo) is inhibited by the female meiosis-specific protein Matrimo
50 analogue 2-heptyl-4-hydroxyquinoline-N-oxide inhibited C. thermarum NDH-2 activity, and its potency i
55 s of DHODH in an enzymatic assay, while also inhibiting cancer cell growth and viability and activati
56 immune regulators and eight chemicals which inhibit Candidatus Liberibacter spp. in plant tissues.
57 rom conserving normal pyroptotic function to inhibiting caspase cleavage to disrupting oligomerizatio
58 1 pre-mixed with HMWHA was more effective in inhibiting catabolic events and stimulating anabolic eve
59 3 also has substantially improved ability to inhibit CCL8, CCL7, CCL2, and CCL3 chemotactic function
60 demonstrates that all antileishmanial drugs inhibit CD4 and CD8 T cell proliferation at the doses th
61 e detergent-resistant membrane domain and to inhibit CD40-induced phosphorylation of the kinases Lyn
62 SD genes activate neural differentiation and inhibit cell cycle during the transition, whereas epilep
64 functions as a serine/threonine kinase that inhibits cell growth, while the HipB antitoxin neutraliz
65 G-CoA reductase inhibitors that are known to inhibit cellular cholesterol biosynthesis and are clinic
66 We hypothesized that dipyridamole, which inhibits cellular adenosine uptake, could raise the extr
67 , binds Tau with low nanomolar affinity, and inhibits cellular Tau aggregate propagation similarly to
69 humans and can act as anti-cancer agents to inhibit chemotherapy-resistant tumor growth by consuming
73 regulatory proteins (p21(Cip1) /p27(Kip1) ) inhibit cyclin and cyclin-dependent kinase (CDK) complex
75 the GNP-glycans can potently and completely inhibit DC-SIGN-mediated augmentation of Ebola virus gly
76 in MCF10A H-RAS(V12) breast cancer cells by inhibiting de novo proline biosynthesis and impairing sp
79 K2 that blocked IL-23 signaling in vitro and inhibited disease progression in animal models of SpA.
81 otentiating radiotherapy and chemotherapy by inhibiting DNA damage repair is proposed as a therapeuti
82 We also assessed the ability of cocaine to inhibit dopamine uptake in the nucleus accumbens core us
83 obic polymer that was extremely effective at inhibiting drug crystallization, and a less effective, b
87 Friend virus (FV) model, Tregs are known to inhibit effector CD8+ T-cell responses and contribute to
88 The addition of latrunculin A to acutely inhibit endocytosis shows that rcy1Delta and snx4Delta s
89 molecules have been classically developed to inhibit enzyme activity; however, new classes of small m
90 enhanced eosinophil spreading on VCAM-1 but inhibited eotaxin-1 (CCL11)-mediated eosinophil migratio
92 sociated with improved task performance, and inhibiting eye movements in humans impaired navigation p
97 behaviour and the timing of reproduction can inhibit genetic exchange between closely related species
99 Pure L. murinus conditioned culture medium inhibited growth and reduced the extension of pneumococc
101 nts with immunodeficient mice, mAb treatment inhibited growth of mutant TP53, WT PTEN LN-229 tumors,
106 but whether bacterial cell wall constituents inhibit HCO(3) transport in the outer medullary collecti
107 glacial and landslide damming in this region inhibited headward propagation of river incision into th
108 a lethal dose of venomous PLA2, L&K-NPs also inhibit hemolysis and confer a significant survival bene
110 o identify HIV-1-suppressing agents that can inhibit HIV-1 reactivation and reduce HIV-1-induced immu
115 ly bound to native and venomous agent X (VX)-inhibited human AChE, here we created seven uncharged ac
118 During studies with the hydroxylase, factor inhibiting hypoxia-inducible factor 1 (FIH-1), we observ
119 plays a key role in the PPP5C-FKBP51 axis to inhibit I(SOC) and protect the endothelial barrier again
120 nous Src tyrosine kinase that constitutively inhibits I(Kv1.5) Disrupting the Src-binding motif of Kv
121 mAbs displayed broad and potent capacity to inhibit IBV NA enzymatic activity, neutralize the virus
125 y ill patients, we showed that mitophagy was inhibited in blood monocytes of patients with sepsis as
126 including nonsense-mediated decay (NMD), are inhibited in c9ALS/FTD brains and in cultured cells expr
127 h yield growth of carbon nanotubes (CNTs) is inhibited in electrolytes containing over 50 wt% of sodi
129 re, we investigated the ability of soy PG to inhibit inflammatory mediator expression in response to
130 tory T cell-inducing molecule retinoic acid, inhibiting inflammatory cytokine production, and making
133 which led to STING carbonylation at C88 and inhibited its trafficking from the endoplasmic reticulum
135 n through regulation of its promoters and by inhibiting its presentation through interaction with the
136 TTR binds Abeta, alters its aggregation, and inhibits its toxicity both in vitro and in vivo In this
137 f the O-fucose site on EGF12 allowed LFNG to inhibit JAG1-NOTCH2 activation, and O-fucosylation on EG
138 TRADD modulates cellular homeostasis by inhibiting K63-linked ubiquitination of beclin 1 mediate
139 reas phosphorylation at the other sites only inhibits Katanin ATPase activity stimulated by MTs.
140 Treatment of HFD-fed mice with verteporfin inhibited KC activation, reduced liver inflammation, and
141 ore the therapeutic potential of transiently inhibiting LDH during adoptive T cell-based immunotherap
142 LIN28B or a LIN28B mutant that is unable to inhibit let-7 processing increases the penetrance of MYC
143 arency results from structural partial order inhibiting light scattering, while preserving mechanical
148 atal testosterone and low prenatal oestrogen inhibits lung development and may predispose individuals
150 lec-8 antibody that depletes eosinophils and inhibits mast cells and that has shown potential in anim
152 ng the series, FCW34 and FCW66 were shown to inhibit MDA-MB-231 cell migration as effectively as ST3G
154 ition and endothelin receptor antagonization inhibited mesenchymal lineage conversion in TGFbeta1-exp
155 stasis suppressor, a class of proteins which inhibits metastatic spread of cancer cells without impac
157 ed genetic manipulations and pharmacology to inhibit MNK-eIF4E activity in animals with spared nerve
158 omas on MNT for survival suggests that drugs inhibiting MNT could significantly boost therapy of MYC-
162 l-regulated kinase pathway inhibition and to inhibit myeloid-derived suppressor cells in various mela
165 endogenous bile acid lithocholic acid (LCA) inhibits NAPE-PLD activity (with an IC(50) of 68 mum), b
169 the prefrontal region during REM sleep, and inhibited neural activation in the untrained region in e
172 se compounds reduces neutrophil velocity and inhibits neutrophil recruitment in response to inflammat
173 5 and dominant-negative mutant IkappaBalphaM inhibited NF-kappaB activity and increased P-p53, p53, a
174 viral activity, we show that PG specifically inhibits NF-kappaB and Akt signaling pathways and promot
177 of different classes and either stimulate or inhibit nucleotide exchange depending on the G-protein s
178 e acceleration observed for Galpha(i), DAPLE inhibited nucleotide exchange on Galpha(s) and Galpha(q)
183 tiple protein kinases that either promote or inhibit origin activation, which is important for genome
187 mall molecule inhibitor, pifithrin-alpha, to inhibit p53 signaling, and nutlin-3a, a small molecule i
188 nistically, CXorf67 interacts with PALB2 and inhibits PALB2-BRCA2 interaction, thereby inhibiting HR
189 phonylureas, widely prescribed for diabetes, inhibit pancreatic ATP-sensitive K(+) (K(ATP) ) channels
190 ngiogenic stimuli to anti-VEGF agents, which inhibit pathologic angiogenesis but also extend normal i
191 targeting PKC with pharmacological tools to inhibit pathologic fibrosis has not been fully evaluated
194 To examine the ability of each antibody to inhibit phagocytosis of platelets, the antibodies were u
195 concentrations of S1P in vitro In addition, inhibiting phospholipase A2 (PLA2) or lipoxygenase (Lox)
196 phosphorylation in one protomer of the dimer inhibits phosphorylation in the second protomer, leading
197 (ZmPTPN) promoted, while knockdown of ZmPTPN inhibited plant drought tolerance, indicating conserved
198 mosquito vectors of the disease, ivermectin inhibits Plasmodium falciparum sporogonic and blood stag
199 XCR5IFN-gammaCD8 T-cell subset significantly inhibits posttransplant alloantibody production in a mur
200 er to show that while depletion of DeltaNp63 inhibits primary mammary adenocarcinoma development, osc
201 s in this procedure, saccades and blinks are inhibited prior to predictable relative to unpredictable
202 Early evidence suggested that actinonin inhibited prokaryote-like post-translational modificatio
204 or shRNA-mediated functional ABCB5 blockade inhibited proliferation and survival of GBM cells and se
205 bsent in the dentate gyrus, which was due to inhibited proliferation of neural stem cells (NSCs).
209 valonate biosynthesis inhibitor, selectively inhibited protein prenylation and induced apoptosis in M
211 Plant cell wall-associated polygalacturonase-inhibiting proteins (PGIPs) are widely distributed in th
213 d linker, the first molecule to successfully inhibit PTP activity through degradation has been develo
214 ethionine, lipid, and purine metabolism, and inhibited quiescence, which explains the life span short
216 st of the prostaglandin D2 receptor that may inhibit recruitment and activation of airway eosinophils
217 specifically projecting to VLO significantly inhibited respiratory responses evoked by inhalation of
219 tion and recruitment of Myo9b, which locally inhibits Rho activity to enhance directional cell migrat
220 ration enhancing and the other configuration inhibiting RNA unwinding compared with the unconstrained
222 tion, we showed that this miRNA specifically inhibits Salmonella infection via modulation of endolyso
223 ation of potential therapies and vaccines to inhibit SARS-CoV-2 infection and ameliorate disease is t
224 d Azithromycin were confirmed to effectively inhibit SARS-CoV-2 replication in vitro with EC50 values
227 neered single-chain variable fragment (scFv) inhibited seeding by IL15-induced tau oligomers and path
228 ween pain catastrophizing and the ability to inhibit selective attention to pain-related faces (atten
229 ecursor UDP-glucuronic acid is sufficient to inhibit several mesenchymal-like properties including ce
232 iamycin-resistant BC cells, while adriamycin inhibited SM-164-resistant BC cell growth, similar to pa
238 h its receptor programmed cell death 1 (PD1) inhibits T cell responses, and blockade of this interact
241 hibited tECM-driven TGFBR2 expression, while inhibiting TGF-beta signaling decreased tECM-mediated ex
242 urface presentation of HLA proteins known to inhibit the activation of an immune cell known as a natu
243 reatment of acute myelogenous leukemia (AML) inhibit the activity of the mammalian topoisomerase II (
246 n intermediate insulation layers are used to inhibit the charge transfer(5,6) or when off-resonance e
248 -quinidine conjugate retained its ability to inhibit the function of P-gp (log IC(50) of 4.20 nM for
250 Furthermore, both VEGF and NRP-1 knockdown inhibit the growth of patient-derived GBM xenografts in
251 present study shows that TA and EGCG do not inhibit the phospholipid-scrambling or ion conduction ac
252 ten use elongation inhibitors to purportedly inhibit the release of puromycin-labeled nascent peptide
253 (NRP-1) attenuate cancer stem cell markers, inhibit the tumor-initiating cell's neurosphere-forming
254 ), we showed that the efflux agonist did not inhibit the uptake of extracellular leucine but instead
255 nd genetic knockdown of SREBP1 significantly inhibited the cell proliferation of mutant KRAS-expressi
257 rther analyses revealed that beta-rubromycin inhibited the germination of cysts and oospores in Pythi
258 interfering with the mTORC1/4E-BP/eIF4E axis inhibited the growth potential endowed by accumulation o
259 blockage of nSMase in monocytes/macrophages inhibited the secretion of inflammatory mediators IL-1be
260 mmune lymphocytes halted LVS replication and inhibited the spread of LVS infection between macrophage
261 In liquid assay system, both GO and MGO inhibited the target bacteria at concentrations signific
262 lf, here we have examined the feasibility of inhibiting the Hsp70 co-chaperone DNAJA1 as a novel anti
265 surface iridium sites, whilst significantly inhibiting the surface cation corrosion during electroca
266 f TPPP1 by EBV-miRNA-BART12, which, in turn, inhibits the acetylation of alpha-tubulin, and promotes
267 cal oligomer concentrations, the interaction inhibits the autocatalytic proliferation of amyloid fibr
270 type I interferon signaling pathway Tyk2 and inhibits the expression of genes induced by type I inter
272 r response machinery but also simultaneously inhibits the STAT3-induced cancer cell proliferation, de
278 and germination and describes strategies for inhibiting these processes to prevent C. difficile infec
283 any bacterial small RNAs (sRNAs) efficiently inhibit translation of target mRNAs by forming a duplex
285 microvascular endothelial cell interactions, inhibited tube stability, and disrupted endothelial cell
286 ciation constant (K(d)) 0.4 +/- 0.1 muM] and inhibits tubulin polymerization in vitro; 4) had no effe
287 s ability to downregulate c-MYC and directly inhibit tumor cell proliferation, NHWD-870 blocks the pr
288 AF3IP2 is more effective; targeting TRAF3IP2 inhibited tumor formation, regressed preformed tumors, a
289 hat while silencing Rab27a and TRAF3IP2 each inhibited tumor growth and metastasis, silencing TRAF3IP
290 care should include bone-targeted agents to inhibit tumour-associated osteolysis and prevent skeleta
291 Moreover, the capability of caftaric acid to inhibit tyrosinase activity was evaluated by spectrophot
295 and Drug Administration-approved drugs that inhibit viral entry, endocytosis, genome assembly, trans
296 a live challenge with RSV infection but was inhibited when BMDCs were treated with GSK J4 prior to s
299 nd, LQZ-7, and when given orally effectively inhibits xenograft tumor growth and induces survivin los